Dynamic and Reprocessable Fluorinated Poly(hindered urea) Network Materials Containing Ionic Liquids to Enhance Triboelectric Performance
- Authors
- Nellepalli, Pothanagandhi; Kim, Minsoo P.; Park, Junyoung; Noh, Seung Man; Ye, Zhibin; Jung, Hyun Wook; Ko, Hyunhyub; Oh, Jung Kwon
- Issue Date
- 20-4월-2022
- Publisher
- AMER CHEMICAL SOC
- Keywords
- dynamic/reversible chemistries; poly(hindered urea); fluorinated polymer network; triboelectric nanogenerator; ionic liquids; self-healability; reprocessability
- Citation
- ACS APPLIED MATERIALS & INTERFACES, v.14, no.15, pp.17806 - 17817
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACS APPLIED MATERIALS & INTERFACES
- Volume
- 14
- Number
- 15
- Start Page
- 17806
- End Page
- 17817
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/142283
- DOI
- 10.1021/acsami.2c01963
- ISSN
- 1944-8244
- Abstract
- Triboelectric nanogenerators (TENGs), a newly developed energy harvesting device that converts surrounding environmental mechanical stimuli into electricity, have been significantly explored as an ideal long-term power source for electrical devices. Despite recent advances, the development of advanced TENG devices with sufficient outputs to sustainably power electronic devices and rapid self-healability under mild conditions to improve their lifetime and function is highly demanded. Here, we report a robust self-healable and reprocessable TENG fabricated with a covalent adaptive network based on mechanically strong fluorinated poly(hindered urea) (F-PHU) integrated with ionic liquid as an efficient dielectric material to improve its triboelectric efficiency and self-healing capability simultaneously. The synthesis and integration of a well-defined reactive copolymer having both pendant fluorinated and t-butylamino bulky groups are the key to fabricate robust F-PHU networks containing fluorinated dangling chains that can interact with ionic liquids to induce ionic polarization, which raises the dielectric constant and thus increases triboelectric performance. They also are cross-linked with dynamic bulky urea linkages for rapid self-healability and high reprocessability through their reversible exchange reactions at moderate temperatures. The developed ionic F-PHU materials exhibit a high TENG output performance (power density of 173.0 mW/m(2)) as well as high TENG output recovery upon repairing their surface damages. This work demonstrates that such a synergistic design of triboelectric ionic F-PHU materials could have great potential for applications requiring high-performance and long-lasting energy harvesting.
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